TY - JOUR
T1 - An implantable system for long-term assessment of atrial fibrillation substrate in unanesthetized rats exposed to underlying pathological conditions
AU - Klapper-Goldstein, Hadar
AU - Murninkas, Michael
AU - Gillis, Roni
AU - Mulla, Wesam
AU - Levanon, Eran
AU - Elyagon, Sigal
AU - Schuster, Ronen
AU - Danan, Dor
AU - Cohen, Hagit
AU - Etzion, Yoram
N1 - Funding Information: This study was supported by a research grant from the Israel Science Foundation (ISF, 1233/19, YE) and an annual research grant from the Israel Heart Society (2016, YE). The development of the new platinum-iridium based electrode was supported by an internal multidisciplinary grant of Ben-Gurion University of the Negev (YE). The supplemental behavioral experiments were supported by a grant from the Israel Science Foundation (ISF, 1174/14, HC). The authors would like to thank Prof. Moshe Gottlieb, Prof. Roni Shneck, Tamar Shami and Daniella Saar for their contribution to the design of the platinum-iridium based electrode. We also thank Prof. Eli Lewis for help with the analysis of inflammatory cytokines. Publisher Copyright: © 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Atrial fibrillation (AF) is a progressive arrhythmia with underlying mechanisms that are not fully elucidated, partially due to lack of reliable and affordable animal models. Here, we introduce a system for long-term assessment of AF susceptibility (substrate) in ambulatory rats implanted with miniature electrodes on the atrium. Rats were subjected to excessive aldosterone (Aldo) or solvent only (Sham). An additional group was exposed to myocardial infarction (MI). AF substrate was tested two- and four-weeks post implantation and was also compared with implanted rats early post-implantation (Base). Aldo and MI increased the AF substrate and atrial fibrosis. In the MI group only, AF duration was correlated with the level of atrial fibrosis and was inversely correlated with systolic function. Unexpectedly, Shams also developed progressive AF substrate relative to Base individuals. Further studies indicated that serum inflammatory markers (IL-6, TNF-alpha) were not elevated in the shams. In addition, we excluded anxiety\depression due to social-isolation as an AF promoting factor. Finally, enhanced biocompatibility of the atrial electrode did not inhibit the gradual development of AF substrate over a testing period of up to 8 weeks. Overall, we successfully validated the first system for long-term AF substrate testing in ambulatory rats.
AB - Atrial fibrillation (AF) is a progressive arrhythmia with underlying mechanisms that are not fully elucidated, partially due to lack of reliable and affordable animal models. Here, we introduce a system for long-term assessment of AF susceptibility (substrate) in ambulatory rats implanted with miniature electrodes on the atrium. Rats were subjected to excessive aldosterone (Aldo) or solvent only (Sham). An additional group was exposed to myocardial infarction (MI). AF substrate was tested two- and four-weeks post implantation and was also compared with implanted rats early post-implantation (Base). Aldo and MI increased the AF substrate and atrial fibrosis. In the MI group only, AF duration was correlated with the level of atrial fibrosis and was inversely correlated with systolic function. Unexpectedly, Shams also developed progressive AF substrate relative to Base individuals. Further studies indicated that serum inflammatory markers (IL-6, TNF-alpha) were not elevated in the shams. In addition, we excluded anxiety\depression due to social-isolation as an AF promoting factor. Finally, enhanced biocompatibility of the atrial electrode did not inhibit the gradual development of AF substrate over a testing period of up to 8 weeks. Overall, we successfully validated the first system for long-term AF substrate testing in ambulatory rats.
UR - http://www.scopus.com/inward/record.url?scp=85078062639&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41598-020-57528-3
DO - https://doi.org/10.1038/s41598-020-57528-3
M3 - Article
C2 - 31953473
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 553
ER -